-
1
-
-
20744456789
-
Solid phase peptide synthesis. I. The synthesis of a tetrapeptide
-
Merrifield RB,. Solid phase peptide synthesis. I. The synthesis of a tetrapeptide. J. Am. Chem. Soc. 1963; 85: 2149-2154.
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 2149-2154
-
-
Merrifield, R.B.1
-
2
-
-
0001926444
-
Solid-phase peptide synthesis
-
Academic Press: New York.
-
Barany G, Merrifield RB,. Solid-phase peptide synthesis. The Peptides, Vol. 2. Academic Press: New York, 1979; 1-284.
-
(1979)
The Peptides
, vol.2
, pp. 1-284
-
-
Barany, G.1
Merrifield, R.B.2
-
3
-
-
0014675276
-
The total synthesis of an enzyme with ribonuclease A activity
-
Gutte B, Merrifield RB,. The total synthesis of an enzyme with ribonuclease A activity. J. Am. Chem. Soc. 1969; 91: 501-502.
-
(1969)
J. Am. Chem. Soc.
, vol.91
, pp. 501-502
-
-
Gutte, B.1
Merrifield, R.B.2
-
4
-
-
0023889559
-
Chemical synthesis of peptides and proteins
-
Kent SBH,. Chemical synthesis of peptides and proteins. Annu. Rev. Biochem. 1988; 57: 957-989.
-
(1988)
Annu. Rev. Biochem.
, vol.57
, pp. 957-989
-
-
Kent, S.B.H.1
-
5
-
-
0022637226
-
Automated chemical synthesis of a protein growth factor for hematopoietic cells, interleukin-3
-
Clark-Lewis I, Aebersold R, Ziltener H, Schrader JW, Hood LE, Kent SBH,. Automated chemical synthesis of a protein growth factor for hematopoietic cells, interleukin-3. Science 1986; 231: 134-139.
-
(1986)
Science
, vol.231
, pp. 134-139
-
-
Clark-Lewis, I.1
Aebersold, R.2
Ziltener, H.3
Schrader, J.W.4
Hood, L.E.5
Kent, S.B.H.6
-
6
-
-
0027944205
-
Synthesis of proteins by native chemical ligation
-
Dawson PE, Muir TW, Clark-Lewis I, Kent SBH,. Synthesis of proteins by native chemical ligation. Science 1994; 266: 776-779.
-
(1994)
Science
, vol.266
, pp. 776-779
-
-
Dawson, P.E.1
Muir, T.W.2
Clark-Lewis, I.3
Kent, S.B.H.4
-
7
-
-
0033791223
-
Synthesis of native proteins by chemical ligation
-
Dawson PE, Kent SB,. Synthesis of native proteins by chemical ligation. Annu. Rev. Biochem. 2000; 69: 923-960.
-
(2000)
Annu. Rev. Biochem.
, vol.69
, pp. 923-960
-
-
Dawson, P.E.1
Kent, S.B.2
-
8
-
-
0033621158
-
Protein synthesis by native chemical ligation: Expanded scope by using straightforward methodology
-
Hackeng TM, Griffin JH, Dawson PE,. Protein synthesis by native chemical ligation: expanded scope by using straightforward methodology. Proc. Natl. Acad. Sci. U. S. A. 1999; 96: 10068-10073.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 10068-10073
-
-
Hackeng, T.M.1
Griffin, J.H.2
Dawson, P.E.3
-
9
-
-
57549083785
-
Expanding the scope of chemoselective peptide ligations in chemical biology
-
Dirksen A, Dawson PE,. Expanding the scope of chemoselective peptide ligations in chemical biology. Curr. Opin. Chem. Biol. 2008; 12: 760-766.
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 760-766
-
-
Dirksen, A.1
Dawson, P.E.2
-
10
-
-
62449282062
-
Total chemical synthesis of proteins
-
Kent SB,. Total chemical synthesis of proteins. Chem. Soc. Rev. 2009; 38: 338-351.
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 338-351
-
-
Kent, S.B.1
-
11
-
-
0037548053
-
Semisynthesis of proteins by expressed protein ligation
-
Muir TW,. Semisynthesis of proteins by expressed protein ligation. Annu. Rev. Biochem. 2003; 72: 249-289.
-
(2003)
Annu. Rev. Biochem.
, vol.72
, pp. 249-289
-
-
Muir, T.W.1
-
12
-
-
57749121492
-
Chemoselective ligation and modification strategies for peptides and proteins
-
Hackenberger CPR, Schwarzer D,. Chemoselective ligation and modification strategies for peptides and proteins. Angew. Chem. Int. Ed. 2008; 47: 10030-10074.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 10030-10074
-
-
Hackenberger, C.P.R.1
Schwarzer, D.2
-
13
-
-
0141504028
-
Total chemical synthesis of enzymes
-
Kent S,. Total chemical synthesis of enzymes. J. Pept. Sci. 2003; 9: 574-593.
-
(2003)
J. Pept. Sci.
, vol.9
, pp. 574-593
-
-
Kent, S.1
-
14
-
-
5444248441
-
Expanded utility of the native chemical ligation reaction
-
Yeo DSY, Srinivasan R, Chen GYJ, Yao SQ,. Expanded utility of the native chemical ligation reaction. Chem.-Eur. J. 2004; 10: 4664-4672.
-
(2004)
Chem.-Eur. J.
, vol.10
, pp. 4664-4672
-
-
Yeo, D.S.Y.1
Srinivasan, R.2
Chen, G.Y.J.3
Yao, S.Q.4
-
16
-
-
41049091181
-
Extending the scope of native chemical peptide coupling
-
Haase C, Seitz O,. Extending the scope of native chemical peptide coupling. Angew. Chem. Int. Ed. 2008; 47: 1553-1556.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 1553-1556
-
-
Haase, C.1
Seitz, O.2
-
17
-
-
57549083785
-
Expanding the scope of chemoselective peptide ligations in chemical biology
-
Dirksen A, Dawson PE,. Expanding the scope of chemoselective peptide ligations in chemical biology. Curr. Opin. Chem. Biol. 2008; 12: 760-766.
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 760-766
-
-
Dirksen, A.1
Dawson, P.E.2
-
18
-
-
0032401970
-
Chemoselective ligation reactions with proteins, oligosaccharides and cells
-
Lemieux GA, Bertozzi CR,. Chemoselective ligation reactions with proteins, oligosaccharides and cells. Trends Biotechnol. 1998; 16: 506-513.
-
(1998)
Trends Biotechnol.
, vol.16
, pp. 506-513
-
-
Lemieux, G.A.1
Bertozzi, C.R.2
-
19
-
-
0035685801
-
Methods and strategies of peptide ligation
-
Tam JP, Xu J, Eom KD,. Methods and strategies of peptide ligation. Biopolymers 2001; 60: 194-205.
-
(2001)
Biopolymers
, vol.60
, pp. 194-205
-
-
Tam, J.P.1
Xu, J.2
Eom, K.D.3
-
20
-
-
0036462604
-
Synthesis of glycoproteins
-
Davis BG,. Synthesis of glycoproteins. Chem. Rev. 2002; 102: 579-601.
-
(2002)
Chem. Rev.
, vol.102
, pp. 579-601
-
-
Davis, B.G.1
-
22
-
-
72149096309
-
Advances in chemical ligation strategies for the synthesis of glycopeptides and glycoproteins
-
Payne RJ, Wong CH,. Advances in chemical ligation strategies for the synthesis of glycopeptides and glycoproteins. Chem. Commun. 2010; 46: 21-43.
-
(2010)
Chem. Commun.
, vol.46
, pp. 21-43
-
-
Payne, R.J.1
Wong, C.H.2
-
23
-
-
33845310540
-
Evolving strategies for protein synthesis converge on native chemical ligation
-
Macmillan D,. Evolving strategies for protein synthesis converge on native chemical ligation. Angew. Chem. Int. Ed. 2006; 45: 7668-7672.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7668-7672
-
-
Macmillan, D.1
-
24
-
-
84867557912
-
Total chemical synthesis of polypeptides and proteins: Chemistry of ligation techniques and beyond
-
Hemantha HP, Narendra N, Sureshbabu VV,. Total chemical synthesis of polypeptides and proteins: chemistry of ligation techniques and beyond. Tetrahedron 2012; 68: 9491-9537.
-
(2012)
Tetrahedron
, vol.68
, pp. 9491-9537
-
-
Hemantha, H.P.1
Narendra, N.2
Sureshbabu, V.V.3
-
25
-
-
33746299267
-
Kinetically controlled ligation for the convergent chemical synthesis of proteins
-
Bang D, Pentelute BL, Kent SB,. Kinetically controlled ligation for the convergent chemical synthesis of proteins. Angew. Chem. Int. Ed. 2006; 45: 3985-3988.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 3985-3988
-
-
Bang, D.1
Pentelute, B.L.2
Kent, S.B.3
-
26
-
-
0032499752
-
Expressed protein ligation: A general method for protein engineering
-
Muir TW, Sondhi D, Cole PA,. Expressed protein ligation: a general method for protein engineering. Proc. Natl. Acad. Sci. U. S. A. 1998; 95: 6705-6710.
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 6705-6710
-
-
Muir, T.W.1
Sondhi, D.2
Cole, P.A.3
-
27
-
-
0032568924
-
Expressed protein ligation, a novel method for studying protein-protein interactions in transcription
-
Severinov K, Muir TW,. Expressed protein ligation, a novel method for studying protein-protein interactions in transcription. J. Biol. Chem. 1998; 273: 16205-16209.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 16205-16209
-
-
Severinov, K.1
Muir, T.W.2
-
28
-
-
33744529377
-
Protein ligation: An enabling technology for the biophysical analysis of proteins
-
Muralidharan V, Muir TW,. Protein ligation: an enabling technology for the biophysical analysis of proteins. Nat. Methods 2006; 3: 429-438.
-
(2006)
Nat. Methods
, vol.3
, pp. 429-438
-
-
Muralidharan, V.1
Muir, T.W.2
-
29
-
-
0035804493
-
Native chemical ligation using removable N-α-(1-phenyl-2- mercaptoethyl) auxiliaries
-
Botti P, Carrasco MR, Kent SBH,. Native chemical ligation using removable N-α-(1-phenyl-2-mercaptoethyl) auxiliaries. Tetrahedron Lett. 2001; 42: 1831-1833.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 1831-1833
-
-
Botti, P.1
Carrasco, M.R.2
Kent, S.B.H.3
-
30
-
-
0033657692
-
N-α-2-mercaptobenzylamine-assisted chemical ligation
-
Offer J, Dawson PE,. N-α-2-mercaptobenzylamine-assisted chemical ligation. Org. Lett. 2000; 2: 23-26.
-
(2000)
Org. Lett.
, vol.2
, pp. 23-26
-
-
Offer, J.1
Dawson, P.E.2
-
31
-
-
0036570182
-
Extending synthetic access to proteins with a removable acyl transfer auxiliary
-
Offer J, Boddy CNC, Dawson PE,. Extending synthetic access to proteins with a removable acyl transfer auxiliary. J. Am. Chem. Soc. 2002; 124: 4642-4646.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 4642-4646
-
-
Offer, J.1
Boddy, C.N.C.2
Dawson, P.E.3
-
32
-
-
11444255322
-
Rapid synthesis of acyl transfer auxiliaries for cysteine-free native glycopeptide ligation
-
Macmillan D, Anderson DW,. Rapid synthesis of acyl transfer auxiliaries for cysteine-free native glycopeptide ligation. Org. Lett. 2004; 6: 4659-4662.
-
(2004)
Org. Lett.
, vol.6
, pp. 4659-4662
-
-
Macmillan, D.1
Anderson, D.W.2
-
33
-
-
33745263964
-
Building complex glycopeptides: Development of a cysteine-free native chemical ligation protocol
-
Wu B, Chen JH, Warren JD, Chen G, Hua ZH, Danishefsky SJ,. Building complex glycopeptides: development of a cysteine-free native chemical ligation protocol. Angew. Chem. Int. Ed. 2006; 45: 4116-4125.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 4116-4125
-
-
Wu, B.1
Chen, J.H.2
Warren, J.D.3
Chen, G.4
Hua, Z.H.5
Danishefsky, S.J.6
-
34
-
-
77956288502
-
Native chemical ligation with N-α acyl transfer auxiliaries
-
Offer J,. Native chemical ligation with N-α acyl transfer auxiliaries. Biopolymers 2010; 94: 530-541.
-
(2010)
Biopolymers
, vol.94
, pp. 530-541
-
-
Offer, J.1
-
35
-
-
33646597740
-
Sugar-assisted glycopeptide ligation
-
Brik A, Yang YY, Ficht S, Wong CH,. Sugar-assisted glycopeptide ligation. J. Am. Chem. Soc. 2006; 128: 5626-5627.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5626-5627
-
-
Brik, A.1
Yang, Y.Y.2
Ficht, S.3
Wong, C.H.4
-
36
-
-
34547813178
-
Second-generation sugar-assisted ligation: A method for the synthesis of cysteine-containing glycopeptides
-
Ficht S, Payne RJ, Brik A, Wong CH,. Second-generation sugar-assisted ligation: a method for the synthesis of cysteine-containing glycopeptides. Angew. Chem. Int. Ed. 2007; 46: 5975-5979.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 5975-5979
-
-
Ficht, S.1
Payne, R.J.2
Brik, A.3
Wong, C.H.4
-
37
-
-
35948946622
-
Extended sugar-assisted glycopeptide ligations: Development, scope and applications
-
Payne RJ, Ficht S, Tang S, Brik A, Yang YY, Case DA, Wong CH,. Extended sugar-assisted glycopeptide ligations: development, scope and applications. J. Am. Chem. Soc. 2007; 129: 13527-13536.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 13527-13536
-
-
Payne, R.J.1
Ficht, S.2
Tang, S.3
Brik, A.4
Yang, Y.Y.5
Case, D.A.6
Wong, C.H.7
-
38
-
-
34250850156
-
Sugar-assisted glycoprotein synthesis
-
Yang YY, Ficht S, Brik A, Wong CH,. Sugar-assisted glycoprotein synthesis. J. Am. Chem. Soc. 2007; 129: 7690-7701.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 7690-7701
-
-
Yang, Y.Y.1
Ficht, S.2
Brik, A.3
Wong, C.H.4
-
39
-
-
51749114233
-
Sugar-assisted glycopeptide ligation with complex oligosaccharides: Scope and limitations
-
Bennett CS, Dean SM, Payne RJ, Ficht S, Brik A, Wong CH,. Sugar-assisted glycopeptide ligation with complex oligosaccharides: scope and limitations. J. Am. Chem. Soc. 2008; 130: 11945-11952.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 11945-11952
-
-
Bennett, C.S.1
Dean, S.M.2
Payne, R.J.3
Ficht, S.4
Brik, A.5
Wong, C.H.6
-
41
-
-
0033397158
-
Polypeptide synthesis by the thioester method
-
Aimoto S,. Polypeptide synthesis by the thioester method. Biopolymers 1999; 51: 247-265.
-
(1999)
Biopolymers
, vol.51
, pp. 247-265
-
-
Aimoto, S.1
-
42
-
-
37349002953
-
Development of efficient methods for accomplishing cysteine-free peptide and glycopeptide coupling
-
Chen G, Wan Q, Tan Z, Kan C, Hua Z, Ranganathan K, Danishefsky SJ,. Development of efficient methods for accomplishing cysteine-free peptide and glycopeptide coupling. Angew. Chem. Int. Ed. 2007; 119: 7527-7531.
-
(2007)
Angew. Chem. Int. Ed.
, vol.119
, pp. 7527-7531
-
-
Chen, G.1
Wan, Q.2
Tan, Z.3
Kan, C.4
Hua, Z.5
Ranganathan, K.6
Danishefsky, S.J.7
-
43
-
-
46749125397
-
Cysteine-free peptide and glycopeptide ligation by direct aminolysis
-
Payne RJ, Ficht S, Greenberg WA, Wong CH,. Cysteine-free peptide and glycopeptide ligation by direct aminolysis. Angew. Chem. Int. Ed. 2008; 47: 4411-4415.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4411-4415
-
-
Payne, R.J.1
Ficht, S.2
Greenberg, W.A.3
Wong, C.H.4
-
44
-
-
67650422251
-
Phosphate-assisted peptide ligation
-
Thomas GL, Payne RJ,. Phosphate-assisted peptide ligation. Chem. Commun. 2009: 4260-4262.
-
(2009)
Chem. Commun.
, pp. 4260-4262
-
-
Thomas, G.L.1
Payne, R.J.2
-
45
-
-
80052771002
-
Peptide ligations accelerated by N-terminal aspartate and glutamate residues
-
Thomas GL, Hsieh YSY, Chun CKY, Cai ZL, Reimers JR, Payne RJ,. Peptide ligations accelerated by N-terminal aspartate and glutamate residues. Org. Lett. 2011; 13: 4770-4773.
-
(2011)
Org. Lett.
, vol.13
, pp. 4770-4773
-
-
Thomas, G.L.1
Hsieh, Y.S.Y.2
Chun, C.K.Y.3
Cai, Z.L.4
Reimers, J.R.5
Payne, R.J.6
-
46
-
-
0037474648
-
The first synthesis of peptide thioester carrying N-linked core pentasaccharide through modified Fmoc thioester preparation: Synthesis of an N-glycosylated Ig domain of emmprin
-
Hojo H, Haginoya E, Matsumoto Y, Nakahara Y, Nabeshima K, Toole BP, Watanabe Y,. The first synthesis of peptide thioester carrying N-linked core pentasaccharide through modified Fmoc thioester preparation: synthesis of an N-glycosylated Ig domain of emmprin. Tetrahedron Lett. 2003; 44: 2961-2964.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 2961-2964
-
-
Hojo, H.1
Haginoya, E.2
Matsumoto, Y.3
Nakahara, Y.4
Nabeshima, K.5
Toole, B.P.6
Watanabe, Y.7
-
47
-
-
25844459506
-
Chemical synthesis of 23 kDa glycoprotein by repetitive segment condensation: A synthesis of MUC2 basal motif carrying multiple O-GalNAc moieties
-
Hojo H, Matsumoto Y, Nakahara Y, Ito E, Suzuki Y, Suzuki M, Suzuki A, Nakahara Y,. Chemical synthesis of 23 kDa glycoprotein by repetitive segment condensation: a synthesis of MUC2 basal motif carrying multiple O-GalNAc moieties. J. Am. Chem. Soc. 2005; 127: 13720-13725.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13720-13725
-
-
Hojo, H.1
Matsumoto, Y.2
Nakahara, Y.3
Ito, E.4
Suzuki, Y.5
Suzuki, M.6
Suzuki, A.7
Nakahara, Y.8
-
48
-
-
43049120006
-
Application of a novel thioesterification reaction to the synthesis of chemokine CCL27 by the modified thioester method
-
Hojo H, Murasawa Y, Katayama H, Ohira T, Nakahara Y, Nakahara Y,. Application of a novel thioesterification reaction to the synthesis of chemokine CCL27 by the modified thioester method. Org. Biomol. Chem. 2008; 6: 1808-1813.
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 1808-1813
-
-
Hojo, H.1
Murasawa, Y.2
Katayama, H.3
Ohira, T.4
Nakahara, Y.5
Nakahara, Y.6
-
49
-
-
77950308364
-
Chemical synthesis of mouse pro-opiomelanocortin(1-74) by azido-protected glycopeptide ligation via the thioester method
-
Katayama H, Hojo H, Shimizu I, Nakahara Y, Nakahara Y,. Chemical synthesis of mouse pro-opiomelanocortin(1-74) by azido-protected glycopeptide ligation via the thioester method. Org. Biomol. Chem. 2010; 8: 1966-1972.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 1966-1972
-
-
Katayama, H.1
Hojo, H.2
Shimizu, I.3
Nakahara, Y.4
Nakahara, Y.5
-
50
-
-
67849101900
-
Toward homogeneous erythropoietin: Fine tuning of the C-terminal acyl donor in the chemical synthesis of the Cys(29)-Gly(77) glycopeptide domain
-
Yuan Y, Chen J, Wan Q, Tan ZP, Chen G, Kan C, Danishefsky SJ,. Toward homogeneous erythropoietin: fine tuning of the C-terminal acyl donor in the chemical synthesis of the Cys(29)-Gly(77) glycopeptide domain. J. Am. Chem. Soc. 2009; 131: 5432-5437.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5432-5437
-
-
Yuan, Y.1
Chen, J.2
Wan, Q.3
Tan, Z.P.4
Chen, G.5
Kan, C.6
Danishefsky, S.J.7
-
51
-
-
67849092526
-
Toward homogeneous erythropoietin: Non-NCL-based chemical synthesis of the Gln(78)-Arg(166) glycopeptide domain
-
Tan ZP, Shang SY, Halkina T, Yuan Y, Danishefsky SJ,. Toward homogeneous erythropoietin: non-NCL-based chemical synthesis of the Gln(78)-Arg(166) glycopeptide domain. J. Am. Chem. Soc. 2009; 131: 5424-5431.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5424-5431
-
-
Tan, Z.P.1
Shang, S.Y.2
Halkina, T.3
Yuan, Y.4
Danishefsky, S.J.5
-
52
-
-
79951657366
-
Total synthesis of microcin B17 via a fragment condensation approach
-
Thompson RE, Jolliffe KA, Payne RJ,. Total synthesis of microcin B17 via a fragment condensation approach. Org. Lett. 2011; 13 (4): 680-683.
-
(2011)
Org. Lett.
, vol.13
, Issue.4
, pp. 680-683
-
-
Thompson, R.E.1
Jolliffe, K.A.2
Payne, R.J.3
-
53
-
-
84892812825
-
Synthesis of MUC1 glycopeptide thioesters and ligation via direct aminolysis
-
Wilkinson BL, Chun CKY, Payne RJ,. Synthesis of MUC1 glycopeptide thioesters and ligation via direct aminolysis. Pept. Sci. 2011; 18: 147-154.
-
(2011)
Pept. Sci.
, vol.18
, pp. 147-154
-
-
Wilkinson, B.L.1
Chun, C.K.Y.2
Payne, R.J.3
-
54
-
-
0035977638
-
Synthesis of peptides and proteins without cysteine residues by native chemical ligation combined with desulfurization
-
Yan LZ, Dawson PE,. Synthesis of peptides and proteins without cysteine residues by native chemical ligation combined with desulfurization. J. Am. Chem. Soc. 2001; 123: 526-533.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 526-533
-
-
Yan, L.Z.1
Dawson, P.E.2
-
56
-
-
37349094422
-
Free-radical-based, specific desulfurization of cysteine: A powerful advance in the synthesis of polypeptides and glycopolypeptides
-
Wan Q, Danishefsky SJ,. Free-radical-based, specific desulfurization of cysteine: a powerful advance in the synthesis of polypeptides and glycopolypeptides. Angew. Chem. Int. Ed. 2007; 46: 9248-9252.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 9248-9252
-
-
Wan, Q.1
Danishefsky, S.J.2
-
57
-
-
0000037978
-
The desulfurization of mercaptans with trialkyl phosphites
-
Hoffmann FW, Ess RJ, Simmons TC, Hanzel RS,. The desulfurization of mercaptans with trialkyl phosphites. J. Am. Chem. Soc. 1956; 78: 6414-6414.
-
(1956)
J. Am. Chem. Soc.
, vol.78
, pp. 6414-6414
-
-
Hoffmann, F.W.1
Ess, R.J.2
Simmons, T.C.3
Hanzel, R.S.4
-
58
-
-
84860830573
-
Probing the stability of nonglycosylated wild-type erythropoietin protein via reiterative alanine ligations
-
Brailsford JA, Danishefsky SJ,. Probing the stability of nonglycosylated wild-type erythropoietin protein via reiterative alanine ligations. Proc. Natl. Acad. Sci. U. S. A. 2012; 109: 7196-7201.
-
(2012)
Proc. Natl. Acad. Sci. U. S. A.
, vol.109
, pp. 7196-7201
-
-
Brailsford, J.A.1
Danishefsky, S.J.2
-
59
-
-
84859540284
-
Total synthesis of homogeneous antifreeze glycopeptides and glycoproteins
-
Wilkinson BL, Stone RS, Capicciotti CJ, Thaysen-Andersen M, Matthews JM, Packer NH, Ben RN, Payne RJ,. Total synthesis of homogeneous antifreeze glycopeptides and glycoproteins. Angew. Chem. Int. Ed. 2012; 51: 3606-3610.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 3606-3610
-
-
Wilkinson, B.L.1
Stone, R.S.2
Capicciotti, C.J.3
Thaysen-Andersen, M.4
Matthews, J.M.5
Packer, N.H.6
Ben, R.N.7
Payne, R.J.8
-
60
-
-
84868547921
-
At last: Erythropoietin as a single glycoform
-
Wang P, Dong S, Brailsford JA, Iyer K, Townsend SD, Zhang Q, Hendrickson RC, Shieh J, Moore MAS, Danishefsky SJ,. At last: erythropoietin as a single glycoform. Angew. Chem. Int. Ed. 2012; 51: 11576-11584.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 11576-11584
-
-
Wang, P.1
Dong, S.2
Brailsford, J.A.3
Iyer, K.4
Townsend, S.D.5
Zhang, Q.6
Hendrickson, R.C.7
Shieh, J.8
Moore, M.A.S.9
Danishefsky, S.J.10
-
61
-
-
84859524073
-
Chemical synthesis of an erythropoietin glycoform containing a complex-type disialyloligosaccharide
-
Murakami M, Okamoto R, Izumi M, Kajihara Y,. Chemical synthesis of an erythropoietin glycoform containing a complex-type disialyloligosaccharide. Angew. Chem. Int. Ed. 2012; 51: 3567-3572.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 3567-3572
-
-
Murakami, M.1
Okamoto, R.2
Izumi, M.3
Kajihara, Y.4
-
62
-
-
84859143910
-
Chemical synthesis of homogeneous human glycosyl-interferon-β that exhibits potent antitumor activity in vivo
-
Sakamoto I, Tezuka K, Fukae K, Ishii K, Taduru K, Maeda M, Ouchi M, Yoshida K, Nambu Y, Igarashi J, Hayashi N, Tsuji T, Kajihara Y,. Chemical synthesis of homogeneous human glycosyl-interferon-β that exhibits potent antitumor activity in vivo. J. Am. Chem. Soc. 2012; 134: 5428-5431.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 5428-5431
-
-
Sakamoto, I.1
Tezuka, K.2
Fukae, K.3
Ishii, K.4
Taduru, K.5
Maeda, M.6
Ouchi, M.7
Yoshida, K.8
Nambu, Y.9
Igarashi, J.10
Hayashi, N.11
Tsuji, T.12
Kajihara, Y.13
-
64
-
-
79954987530
-
Chemical synthesis and expression of the HIV-1 Rev protein
-
Siman P, Blatt O, Moyal T, Danieli T, Lebendiker M, Lashuel HA, Friedler A, Brik A,. Chemical synthesis and expression of the HIV-1 Rev protein. ChemBioChem 2011; 12: 1097-1104.
-
(2011)
ChemBioChem
, vol.12
, pp. 1097-1104
-
-
Siman, P.1
Blatt, O.2
Moyal, T.3
Danieli, T.4
Lebendiker, M.5
Lashuel, H.A.6
Friedler, A.7
Brik, A.8
-
65
-
-
80355130228
-
Native chemical ligation combined with desulfurization and deselenization: A general strategy for chemical protein synthesis
-
Dawson PE,. Native chemical ligation combined with desulfurization and deselenization: a general strategy for chemical protein synthesis. Isr. J. Chem. 2011; 51: 862-867.
-
(2011)
Isr. J. Chem.
, vol.51
, pp. 862-867
-
-
Dawson, P.E.1
-
66
-
-
34548153495
-
Native chemical ligation at phenylalanine
-
Crich D, Banerjee A,. Native chemical ligation at phenylalanine. J. Am. Chem. Soc. 2007; 129: 10064-10065.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 10064-10065
-
-
Crich, D.1
Banerjee, A.2
-
67
-
-
54249149331
-
Native chemical ligation at valine: A contribution to peptide and glycopeptide synthesis
-
Chen J, Wan Q, Yuan Y, Zhu JL, Danishefsky SJ,. Native chemical ligation at valine: a contribution to peptide and glycopeptide synthesis. Angew. Chem. Int. Ed. 2008; 47: 8521-8524.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 8521-8524
-
-
Chen, J.1
Wan, Q.2
Yuan, Y.3
Zhu, J.L.4
Danishefsky, S.J.5
-
68
-
-
70349974584
-
Highly efficient and chemoselective peptide ubiquitylation
-
Ajish Kumar KS, Haj-Yahya M, Olschewski D, Lashuel HA, Brik A,. Highly efficient and chemoselective peptide ubiquitylation. Angew. Chem. Int. Ed. 2009; 48: 8090-8094.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 8090-8094
-
-
Ajish Kumar, K.S.1
Haj-Yahya, M.2
Olschewski, D.3
Lashuel, H.A.4
Brik, A.5
-
69
-
-
70349754425
-
Dual native chemical ligation at lysine
-
Yang RL, Pasunooti KK, Li FP, Liu XW, Liu CF,. Dual native chemical ligation at lysine. J. Am. Chem. Soc. 2009; 131: 13592-13593.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 13592-13593
-
-
Yang, R.L.1
Pasunooti, K.K.2
Li, F.P.3
Liu, X.W.4
Liu, C.F.5
-
70
-
-
78650446183
-
Chemical synthesis of ubiquitin, ubiquitin-based probes, and diubiquitin
-
El Oualid F, Merkx R, Ekkebus R, Hameed DS, Smit JJ, de Jong A, Hilkmann H, Sixma TK, Ovaa H,. Chemical synthesis of ubiquitin, ubiquitin-based probes, and diubiquitin. Angew. Chem. Int. Ed. 2010; 49: 10149-10153.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 10149-10153
-
-
El Oualid, F.1
Merkx, R.2
Ekkebus, R.3
Hameed, D.S.4
Smit, J.J.5
De Jong, A.6
Hilkmann, H.7
Sixma, T.K.8
Ovaa, H.9
-
71
-
-
77953463939
-
Protein synthesis assisted by native chemical ligation at leucine
-
Harpaz Z, Siman P, Kumar KSA, Brik A,. Protein synthesis assisted by native chemical ligation at leucine. ChemBioChem 2010; 11: 1232-1235.
-
(2010)
ChemBioChem
, vol.11
, pp. 1232-1235
-
-
Harpaz, Z.1
Siman, P.2
Kumar, K.S.A.3
Brik, A.4
-
72
-
-
78650159619
-
Insights into the finer issues of native chemical ligation: An approach to cascade ligations
-
Tan ZP, Shang SY, Danishefsky SJ,. Insights into the finer issues of native chemical ligation: an approach to cascade ligations. Angew. Chem. Int. Ed. 2010; 49: 9500-9503.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 9500-9503
-
-
Tan, Z.P.1
Shang, S.Y.2
Danishefsky, S.J.3
-
73
-
-
79960228639
-
An advance in proline ligation
-
Shang SY, Tan ZP, Dong SW, Danishefsky SJ,. An advance in proline ligation. J. Am. Chem. Soc. 2011; 133: 10784-10786.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10784-10786
-
-
Shang, S.Y.1
Tan, Z.P.2
Dong, S.W.3
Danishefsky, S.J.4
-
74
-
-
80054694198
-
Dual kinetically controlled native chemical ligation using a combination of sulfanylproline and sulfanylethylanilide peptide
-
Ding H, Shigenaga A, Sato K, Morishita K, Otaka A,. Dual kinetically controlled native chemical ligation using a combination of sulfanylproline and sulfanylethylanilide peptide. Org. Lett. 2011; 13: 5588-5591.
-
(2011)
Org. Lett.
, vol.13
, pp. 5588-5591
-
-
Ding, H.1
Shigenaga, A.2
Sato, K.3
Morishita, K.4
Otaka, A.5
-
75
-
-
77649190705
-
A program for ligation at threonine sites: Application to the controlled total synthesis of glycopeptides
-
Chen J, Wang P, Zhu JL, Wan Q, Danishefsky SJ,. A program for ligation at threonine sites: application to the controlled total synthesis of glycopeptides. Tetrahedron 2010; 66: 2277-2283.
-
(2010)
Tetrahedron
, vol.66
, pp. 2277-2283
-
-
Chen, J.1
Wang, P.2
Zhu, J.L.3
Wan, Q.4
Danishefsky, S.J.5
-
76
-
-
84875002264
-
Peptide ligation-desulfurization chemistry at arginine
-
Malins LR, Cergol KM, Payne RJ,. Peptide ligation-desulfurization chemistry at arginine. ChemBioChem 2013; 14: 559-563.
-
(2013)
ChemBioChem
, vol.14
, pp. 559-563
-
-
Malins, L.R.1
Cergol, K.M.2
Payne, R.J.3
-
77
-
-
84892832674
-
Chemoselective peptide ligation-desulfurization at aspartate
-
Thompson RE, Chan B, Radom L, Jolliffe KA, Payne RJ,. Chemoselective peptide ligation-desulfurization at aspartate. Angew. Chem. Int. Ed. 2013; 14: 559-563.
-
(2013)
Angew. Chem. Int. Ed.
, vol.14
, pp. 559-563
-
-
Thompson, R.E.1
Chan, B.2
Radom, L.3
Jolliffe, K.A.4
Payne, R.J.5
-
78
-
-
84888625825
-
Chemoselective sulfenylation and peptide ligation at tryptophan
-
Malins LR, Cergol KM, Payne RJ,. Chemoselective sulfenylation and peptide ligation at tryptophan. Chem. Sci. 2014; 5 (1): 260-266.
-
(2014)
Chem. Sci.
, vol.5
, Issue.1
, pp. 260-266
-
-
Malins, L.R.1
Cergol, K.M.2
Payne, R.J.3
-
79
-
-
33847791752
-
Selective desulfurization of cysteine in the presence of Cys(Acm) in polypeptides obtained by native chemical ligation
-
Pentelute BL, Kent SBH,. Selective desulfurization of cysteine in the presence of Cys(Acm) in polypeptides obtained by native chemical ligation. Org. Lett. 2007; 9: 687-690.
-
(2007)
Org. Lett.
, vol.9
, pp. 687-690
-
-
Pentelute, B.L.1
Kent, S.B.H.2
-
80
-
-
0034995886
-
Selenocysteine-mediated native chemical ligation
-
Quaderer R, Sewing A, Hilvert D,. Selenocysteine-mediated native chemical ligation. Helv. Chim. Acta 2001; 84: 1197-1206.
-
(2001)
Helv. Chim. Acta
, vol.84
, pp. 1197-1206
-
-
Quaderer, R.1
Sewing, A.2
Hilvert, D.3
-
81
-
-
0035799867
-
Synthesis of a selenocysteine-containing peptide by native chemical ligation
-
Gieselman MD, Xie L, van Der Donk WA,. Synthesis of a selenocysteine-containing peptide by native chemical ligation. Org. Lett. 2001; 3: 1331-1334.
-
(2001)
Org. Lett.
, vol.3
, pp. 1331-1334
-
-
Gieselman, M.D.1
Xie, L.2
Van Der Donk, W.A.3
-
82
-
-
0034808792
-
Selenocysteine in native chemical ligation and expressed protein ligation
-
Hondal RJ, Nilsson BL, Raines RT,. Selenocysteine in native chemical ligation and expressed protein ligation. J. Am. Chem. Soc. 2001; 123: 5140-5141.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5140-5141
-
-
Hondal, R.J.1
Nilsson, B.L.2
Raines, R.T.3
-
83
-
-
77956909658
-
Traceless ligation of cysteine peptides using selective deselenization
-
Metanis N, Keinan E, Dawson PE,. Traceless ligation of cysteine peptides using selective deselenization. Angew. Chem. Int. Ed. 2010; 49: 7049-7053.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 7049-7053
-
-
Metanis, N.1
Keinan, E.2
Dawson, P.E.3
-
84
-
-
1842388071
-
Selenium as an integral part of factor 3 against dietary necrotic liver degeneration
-
Schwarz K, Foltz CM,. Selenium as an integral part of factor 3 against dietary necrotic liver degeneration. J. Am. Chem. Soc. 1957; 79: 3292-3293.
-
(1957)
J. Am. Chem. Soc.
, vol.79
, pp. 3292-3293
-
-
Schwarz, K.1
Foltz, C.M.2
-
88
-
-
27144469008
-
Selenocysteine in proteins - Properties and biotechnological use
-
Johansson L, Gafvelin G, Arner ESJ,. Selenocysteine in proteins-properties and biotechnological use. Biochim. Biophys. Acta, Gen. Subj. 2005; 1726: 1-13.
-
(2005)
Biochim. Biophys. Acta, Gen. Subj.
, vol.1726
, pp. 1-13
-
-
Johansson, L.1
Gafvelin, G.2
Arner, E.S.J.3
-
89
-
-
0001398071
-
Chemical characterization of the selenoprotein component of clostridial glycine reductase: Identification of selenocysteine as the organoselenium moiety
-
Cone JE, Martin DRR, Davis JN, Stadtman TC,. Chemical characterization of the selenoprotein component of clostridial glycine reductase: identification of selenocysteine as the organoselenium moiety. Proc. Natl. Acad. Sci. U. S. A. 1976; 73: 2659-2663.
-
(1976)
Proc. Natl. Acad. Sci. U. S. A.
, vol.73
, pp. 2659-2663
-
-
Cone, J.E.1
Martin, D.R.R.2
Davis, J.N.3
Stadtman, T.C.4
-
90
-
-
0025963803
-
Selenocysteine: The 21st amino acid
-
Bock A, Forchhammer K, Heider J, Leinfelder W, Sawers G, Veprek B, Zinoni F,. Selenocysteine: the 21st amino acid. Mol. Microbiol. 1991; 5: 515-520.
-
(1991)
Mol. Microbiol.
, vol.5
, pp. 515-520
-
-
Bock, A.1
Forchhammer, K.2
Heider, J.3
Leinfelder, W.4
Sawers, G.5
Veprek, B.6
Zinoni, F.7
-
91
-
-
0034705133
-
Structure and mechanism of mammalian thioredoxin reductase: The active site is a redox-active selenolthiol/selenenylsulfide formed from the conserved cysteine-selenocysteine sequence
-
Zhong L, Arnér ESJ, Holmgren A,. Structure and mechanism of mammalian thioredoxin reductase: the active site is a redox-active selenolthiol/selenenylsulfide formed from the conserved cysteine-selenocysteine sequence. Proc. Natl. Acad. Sci. U. S. A. 2000; 97: 5854-5859.
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 5854-5859
-
-
Zhong, L.1
Arnér, E.S.J.2
Holmgren, A.3
-
92
-
-
0034646457
-
Mammalian thioredoxin reductase: Oxidation of the C-terminal cysteine/selenocysteine active site forms a thioselenide, and replacement of selenium with sulfur markedly reduces catalytic activity
-
Lee SR, Bar Noy S, Kwon J, Levine RL, Stadtman TC, Rhee SG,. Mammalian thioredoxin reductase: oxidation of the C-terminal cysteine/selenocysteine active site forms a thioselenide, and replacement of selenium with sulfur markedly reduces catalytic activity. Proc. Natl. Acad. Sci. U. S. A. 2000; 97: 2521-2526.
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 2521-2526
-
-
Lee, S.R.1
Bar Noy, S.2
Kwon, J.3
Levine, R.L.4
Stadtman, T.C.5
Rhee, S.G.6
-
93
-
-
0025996978
-
Catalytic properties of an Escherichia coli formate dehydrogenase mutant in which sulfur replaces selenium
-
Axley MJ, Böck A, Stadtman TC,. Catalytic properties of an Escherichia coli formate dehydrogenase mutant in which sulfur replaces selenium. Proc. Natl. Acad. Sci. U. S. A. 1991; 88: 8450-8454.
-
(1991)
Proc. Natl. Acad. Sci. U. S. A.
, vol.88
, pp. 8450-8454
-
-
Axley, M.J.1
Böck, A.2
Stadtman, T.C.3
-
94
-
-
0000210110
-
Nuclear magnetic resonance studies of the solution chemistry of metal complexes. 23. Complexation of methylmercury by selenohydryl-containing amino acids and related molecules
-
Arnold AP, Tan KS, Rabenstein DL,. Nuclear magnetic resonance studies of the solution chemistry of metal complexes. 23. Complexation of methylmercury by selenohydryl-containing amino acids and related molecules. Inorg. Chem. 1986; 25: 2433-2437.
-
(1986)
Inorg. Chem.
, vol.25
, pp. 2433-2437
-
-
Arnold, A.P.1
Tan, K.S.2
Rabenstein, D.L.3
-
95
-
-
0014143854
-
Comparison of the chemical properties of selenocysteine and selenocystine with their sulfur analogs
-
Huber R, Criddle RS,. Comparison of the chemical properties of selenocysteine and selenocystine with their sulfur analogs. Arch. Biochem. Biophys. 1967; 122: 164-173.
-
(1967)
Arch. Biochem. Biophys.
, vol.122
, pp. 164-173
-
-
Huber, R.1
Criddle, R.S.2
-
96
-
-
0030969653
-
The redox potential of selenocystine in unconstrained cyclic peptides
-
Besse D, Siedler F, Diercks T, Kessler H, Moroder L,. The redox potential of selenocystine in unconstrained cyclic peptides. Angew. Chem. Int. Ed. 1997; 36: 883-885.
-
(1997)
Angew. Chem. Int. Ed.
, vol.36
, pp. 883-885
-
-
Besse, D.1
Siedler, F.2
Diercks, T.3
Kessler, H.4
Moroder, L.5
-
97
-
-
33646545095
-
Catalysis of electron transfer by selenocysteine
-
Nauser T, Dockheer S, Kissner R, Koppenol WH,. Catalysis of electron transfer by selenocysteine. Biochemistry 2006; 45: 6038-6043.
-
(2006)
Biochemistry
, vol.45
, pp. 6038-6043
-
-
Nauser, T.1
Dockheer, S.2
Kissner, R.3
Koppenol, W.H.4
-
98
-
-
0001669134
-
Methods in selenium chemistry. III. Reduction of diselenides with dithiothreitol
-
Guenther WHH,. Methods in selenium chemistry. III. Reduction of diselenides with dithiothreitol. J. Org. Chem. 1967; 32: 3931-3934.
-
(1967)
J. Org. Chem.
, vol.32
, pp. 3931-3934
-
-
Guenther, W.H.H.1
-
99
-
-
0032484231
-
Isomorphous replacement of cystine with selenocystine in endothelin: Oxidative refolding, biological and conformational properties of [Sec3,Sec11,Nle7]-endothelin-1
-
Pegoraro S, Fiori S, Rudolph-Böhner S, Watanabe TX, Moroder L,. Isomorphous replacement of cystine with selenocystine in endothelin: oxidative refolding, biological and conformational properties of [Sec3,Sec11,Nle7]- endothelin-1. J. Mol. Biol. 1998; 284: 779-792.
-
(1998)
J. Mol. Biol.
, vol.284
, pp. 779-792
-
-
Pegoraro, S.1
Fiori, S.2
Rudolph-Böhner, S.3
Watanabe, T.X.4
Moroder, L.5
-
100
-
-
0032787875
-
The disulfide-coupled folding pathway of apamin as derived from diselenide-quenched analogs and intermediates
-
Pegoraro S, Fiori S, Cramer J, Rudolph-Böhner S, Moroder L,. The disulfide-coupled folding pathway of apamin as derived from diselenide-quenched analogs and intermediates. Protein Sci. 1999; 8: 1605-1613.
-
(1999)
Protein Sci.
, vol.8
, pp. 1605-1613
-
-
Pegoraro, S.1
Fiori, S.2
Cramer, J.3
Rudolph-Böhner, S.4
Moroder, L.5
-
101
-
-
0034058941
-
Synthesis and conformational analysis of apamin analogues with natural and non-natural cystine/selenocystine connectivities
-
Fiori S, Pegoraro S, Rudolph-Böhner S, Cramer J, Moroder L,. Synthesis and conformational analysis of apamin analogues with natural and non-natural cystine/selenocystine connectivities. Biopolymers 2000; 53: 550-564.
-
(2000)
Biopolymers
, vol.53
, pp. 550-564
-
-
Fiori, S.1
Pegoraro, S.2
Rudolph-Böhner, S.3
Cramer, J.4
Moroder, L.5
-
102
-
-
84861618059
-
Strategic use of non-native diselenide bridges to steer oxidative protein folding
-
Metanis N, Hilvert D,. Strategic use of non-native diselenide bridges to steer oxidative protein folding. Angew. Chem. Int. Ed. 2012; 51: 5585-5588.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 5585-5588
-
-
Metanis, N.1
Hilvert, D.2
-
103
-
-
78650111991
-
Selenopeptide analogs of EETI-II retain potent trypsin inhibitory activities
-
Walewska A, Jaśkiewicz A, Bulaj G, Rolka K,. Selenopeptide analogs of EETI-II retain potent trypsin inhibitory activities. Chem. Biol. Drug Des. 2011; 77: 93-97.
-
(2011)
Chem. Biol. Drug Des.
, vol.77
, pp. 93-97
-
-
Walewska, A.1
Jaśkiewicz, A.2
Bulaj, G.3
Rolka, K.4
-
104
-
-
33744918558
-
α-Selenoconotoxins, a new class of potent α7 neuronal nicotinic receptor antagonists
-
Armishaw CJ, Daly NL, Nevin ST, Adams DJ, Craik DJ, Alewood PF,. α-Selenoconotoxins, a new class of potent α7 neuronal nicotinic receptor antagonists. J. Biol. Chem. 2006; 281: 14136-14143.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 14136-14143
-
-
Armishaw, C.J.1
Daly, N.L.2
Nevin, S.T.3
Adams, D.J.4
Craik, D.J.5
Alewood, P.F.6
-
105
-
-
61949466107
-
Integrated oxidative folding of cysteine/selenocysteine containing peptides: Improving chemical synthesis of conotoxins
-
Walewska A, Zhang M-M, Skalicky JJ, Yoshikami D, Olivera BM, Bulaj G,. Integrated oxidative folding of cysteine/selenocysteine containing peptides: improving chemical synthesis of conotoxins. Angew. Chem. Int. Ed. 2009; 48: 2221-2224.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 2221-2224
-
-
Walewska, A.1
Zhang, M.-M.2
Skalicky, J.J.3
Yoshikami, D.4
Olivera, B.M.5
Bulaj, G.6
-
106
-
-
77949391358
-
Solving the α-conotoxin folding problem: Efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antagonists
-
Muttenthaler M, Nevin ST, Grishin AA, Ngo ST, Choy PT, Daly NL, Hu S-H, Armishaw CJ, Wang C-IA, Lewis RJ, Martin JL, Noakes PG, Craik DJ, Adams DJ, Alewood PF,. Solving the α-conotoxin folding problem: efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antagonists. J. Am. Chem. Soc. 2010; 132: 3514-3522.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 3514-3522
-
-
Muttenthaler, M.1
Nevin, S.T.2
Grishin, A.A.3
Ngo, S.T.4
Choy, P.T.5
Daly, N.L.6
Hu, S.-H.7
Armishaw, C.J.8
Wang, C.-I.9
Lewis, R.J.10
Martin, J.L.11
Noakes, P.G.12
Craik, D.J.13
Adams, D.J.14
Alewood, P.F.15
-
107
-
-
77949820036
-
Site-specific effects of diselenide bridges on the oxidative folding of a cystine knot peptide, ω-selenoconotoxin GVIA
-
Gowd KH, Yarotskyy V, Elmslie KS, Skalicky JJ, Olivera BM, Bulaj G,. Site-specific effects of diselenide bridges on the oxidative folding of a cystine knot peptide, ω-selenoconotoxin GVIA. Biochemistry 2010; 49: 2741-2752.
-
(2010)
Biochemistry
, vol.49
, pp. 2741-2752
-
-
Gowd, K.H.1
Yarotskyy, V.2
Elmslie, K.S.3
Skalicky, J.J.4
Olivera, B.M.5
Bulaj, G.6
-
108
-
-
79959935844
-
Total synthesis of the analgesic conotoxin MrVIB through selenocysteine-assisted folding
-
deâ€...Araujo AD
-
deâ€...Araujo AD, Callaghan B, Nevin ST, Daly NL, Craik DJ, Moretta M, Hopping G, Christie MJ, Adams DJ, Alewood PF,. Total synthesis of the analgesic conotoxin MrVIB through selenocysteine-assisted folding. Angew. Chem. Int. Ed. 2011; 50: 6527-6529.
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 6527-6529
-
-
Callaghan, B.1
Nevin, S.T.2
Daly, N.L.3
Craik, D.J.4
Moretta, M.5
Hopping, G.6
Christie, M.J.7
Adams, D.J.8
Alewood, P.F.9
-
109
-
-
84861583393
-
Reagentless oxidative folding of disulfide-rich peptides catalyzed by an intramolecular diselenide
-
Steiner AM, Woycechowsky KJ, Olivera BM, Bulaj G,. Reagentless oxidative folding of disulfide-rich peptides catalyzed by an intramolecular diselenide. Angew. Chem. Int. Ed. 2012; 51: 5580-5584.
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 5580-5584
-
-
Steiner, A.M.1
Woycechowsky, K.J.2
Olivera, B.M.3
Bulaj, G.4
-
110
-
-
67650729040
-
Chapter 5 expressed protein ligation for metalloprotein design and engineering
-
Clark KM, van der Donk WA, Lu Y,. Chapter 5 expressed protein ligation for metalloprotein design and engineering. Methods Enzymol. 2009; 462: 97-115.
-
(2009)
Methods Enzymol.
, vol.462
, pp. 97-115
-
-
Clark, K.M.1
Van Der Donk, W.A.2
Lu, Y.3
-
111
-
-
0036119701
-
Semisynthesis of proteins containing selenocysteine
-
Hondal RJ, Raines RT,. Semisynthesis of proteins containing selenocysteine. Methods Enzymol. 2002; 347: 70-83.
-
(2002)
Methods Enzymol.
, vol.347
, pp. 70-83
-
-
Hondal, R.J.1
Raines, R.T.2
-
112
-
-
27744456247
-
Incorporation of selenocysteine into proteins using peptide ligation
-
Hondal RJ,. Incorporation of selenocysteine into proteins using peptide ligation. Protein Pept. Lett. 2005; 12: 757-764.
-
(2005)
Protein Pept. Lett.
, vol.12
, pp. 757-764
-
-
Hondal, R.J.1
-
113
-
-
0036905726
-
Selenocysteine derivatives for chemoselective ligations
-
Gieselman MD, Zhu YT, Zhou H, Galonic D, van der Donk WA,. Selenocysteine derivatives for chemoselective ligations. ChemBioChem 2002; 3: 709-716.
-
(2002)
ChemBioChem
, vol.3
, pp. 709-716
-
-
Gieselman, M.D.1
Zhu, Y.T.2
Zhou, H.3
Galonic, D.4
Van Der Donk, W.A.5
-
114
-
-
0036434268
-
Selenocysteine-mediated backbone cyclization of unprotected peptides followed by alkylation, oxidative elimination or reduction of the selenol
-
Quaderer R, Hilvert D,. Selenocysteine-mediated backbone cyclization of unprotected peptides followed by alkylation, oxidative elimination or reduction of the selenol. Chem. Commun. 2002: 2620-2621.
-
(2002)
Chem. Commun.
, pp. 2620-2621
-
-
Quaderer, R.1
Hilvert, D.2
-
115
-
-
0037070614
-
An engineered azurin variant containing a selenocysteine copper ligand
-
Berry SM, Gieselman MD, Nilges MJ, van der Donk WA, Lu Y,. An engineered azurin variant containing a selenocysteine copper ligand. J. Am. Chem. Soc. 2002; 124: 2084-2085.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2084-2085
-
-
Berry, S.M.1
Gieselman, M.D.2
Nilges, M.J.3
Van Der Donk, W.A.4
Lu, Y.5
-
116
-
-
67649130281
-
Chemical modification of proteins at cysteine: Opportunities in chemistry and biology
-
Chalker JM, Bernardes GJL, Lin YA, Davis BG,. Chemical modification of proteins at cysteine: opportunities in chemistry and biology. Chem. Asian J. 2009; 4: 630-640.
-
(2009)
Chem. Asian J.
, vol.4
, pp. 630-640
-
-
Chalker, J.M.1
Bernardes, G.J.L.2
Lin, Y.A.3
Davis, B.G.4
-
117
-
-
80052995647
-
A "tag-and-modify" approach to site-selective protein modification
-
Chalker JM, Bernardes GJL, Davis BG,. A "tag-and-modify" approach to site-selective protein modification. Acc. Chem. Res. 2011; 44: 730-741.
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 730-741
-
-
Chalker, J.M.1
Bernardes, G.J.L.2
Davis, B.G.3
-
118
-
-
0001652407
-
Some extensions of the reaction of trivalent phosphorus derivatives with alkoxy and thiyl radicals; A new synthesis of thioesters
-
Walling C, Basedow OH, Savas ES,. Some extensions of the reaction of trivalent phosphorus derivatives with alkoxy and thiyl radicals; a new synthesis of thioesters. J. Am. Chem. Soc. 1960; 82: 2181-2184.
-
(1960)
J. Am. Chem. Soc.
, vol.82
, pp. 2181-2184
-
-
Walling, C.1
Basedow, O.H.2
Savas, E.S.3
-
119
-
-
84875823571
-
Synthetic cysteine surrogates used in native chemical ligation
-
Wong CTT, Tung CL, Li X,. Synthetic cysteine surrogates used in native chemical ligation. Mol. Biosyst. 2013; 9: 826-833.
-
(2013)
Mol. Biosyst.
, vol.9
, pp. 826-833
-
-
Wong, C.T.T.1
Tung, C.L.2
Li, X.3
-
120
-
-
84857739989
-
Advances in proline ligation
-
Townsend SD, Tan Z, Dong S, Shang S, Brailsford JA, Danishefsky SJ,. Advances in proline ligation. J. Am. Chem. Soc. 2012; 134: 3912-3916.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 3912-3916
-
-
Townsend, S.D.1
Tan, Z.2
Dong, S.3
Shang, S.4
Brailsford, J.A.5
Danishefsky, S.J.6
-
121
-
-
84862536685
-
Synthesis and utility of β-selenol-phenylalanine for native chemical ligation-deselenization chemistry
-
Malins LR, Payne RJ,. Synthesis and utility of β-selenol- phenylalanine for native chemical ligation-deselenization chemistry. Org. Lett. 2012; 14: 3142-3145.
-
(2012)
Org. Lett.
, vol.14
, pp. 3142-3145
-
-
Malins, L.R.1
Payne, R.J.2
-
122
-
-
33847123581
-
Studies on deprotection of cysteine and selenocysteine side-chain protecting groups
-
Harris KM, Flemer S, Hondal RJ,. Studies on deprotection of cysteine and selenocysteine side-chain protecting groups. J. Pept. Sci. 2007; 13: 81-93.
-
(2007)
J. Pept. Sci.
, vol.13
, pp. 81-93
-
-
Harris, K.M.1
Flemer, S.2
Hondal, R.J.3
-
123
-
-
84877762505
-
Highly efficient one-pot ligation and desulfurization
-
Moyal T, Hemantha HP, Siman P, Refua M, Brik A,. Highly efficient one-pot ligation and desulfurization. Chem. Sci. 2013; 4: 2496-2501.
-
(2013)
Chem. Sci.
, vol.4
, pp. 2496-2501
-
-
Moyal, T.1
Hemantha, H.P.2
Siman, P.3
Refua, M.4
Brik, A.5
|